HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → N-[4-(Hydroxymethyl)-1,3-thiazol-2-YL]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2-Acetamido-1,3-thiazol-4-yl)methyl acetate | HCID 14931747 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[4-(Hydroxymethyl)-1,3-thiazol-2-YL]acetamide | HCID 14931748 | 71% |
Reaction Steps
Mass (m/e): 214 (M30) . (2) A mixture of 2-acetylamino-4-acetoxymethylthiazole (72 g), potassium carbonate (23.2 g), methanol (1.1 l) and water (0.1 l) was stirred for 3 hours and 20 minutes at ambient temperature. An insoluble material was filtered off and the filtrate was neutralized with 2N hydrochloric acid and evaporated. To the residue was added a mixture of chloroform and methanol (100 ml, 1:1 V/V) and the mixture was heated. An insoluble material was filtered off and the filtrate was concentrated. The residue was purified by column chromatography on silica gel eluting with a mixture of chloroform and methanol (10:1 V/V) to give 2-acetylamino-4-hydroxymethylthiazole (41.11 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04742057 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-4c7a82f635a342cfa02633bb9fa5d2cb |
| Source note | uspto-grants-1988_05 |